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Newborn screening algorithm distinguishing potential symptomatic isovaleric acidemia from asymptomatic newborns
by
Rock, Rachel
,
Rock, Oded
,
Daas, Suha
,
Biton-Regev, Vered
,
Sagiv, Nadav
,
Salah, Nasser Abu
,
Anikster, Yair
,
Barel, Ortal
,
Cohen, Ronen Hady
,
Dumin, Elena
,
Fattal-Valevski, Aviva
,
Falik-Zaccai, Tzipora
,
Herskovitz, Eli
,
Josefsberg, Sagi
,
Khammash, Hatem
,
Kneller, Katya
,
Korman, Stanley H
,
Landau, Yuval E
,
Lerman-Sagie, Tally
,
Mandel, Hanna
,
Pras, Elon
,
Reznik-Wolf, Haike
,
Shaag, Avraham
,
Lotan, Nava Shaul
,
Spiegel, Ronen
,
Tal, Galit
,
Staretz-Chacham, Orna
,
Wilnai, Yael
,
Almashanu, Shlomo
Published in
Journal of inherited metabolic disease
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Journal Of Inherited Metabolic Disease
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Algorithms
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Amino Acid Metabolism, Inborn Errors - Diagnosis
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Amino Acid Metabolism, Inborn Errors - Genetics
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Endocrinology & Metabolism
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Female
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Genetics & Heredity
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Humans
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Infant, Newborn
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Isovaleryl-Coa Dehydrogenase - Deficiency
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Isovaleryl-Coa Dehydrogenase - Genetics
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Israel
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Life Sciences & Biomedicine
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Male
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Medicine, Research & Experimental
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Neonatal Screening - Methods
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Phenotype
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Research & Experimental Medicine
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Science & Technology
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